Literature DB >> 1716760

Prenatal diagnosis of recurrent Larsen syndrome: further definition of a lethal variant.

D Mostello1, L Hoechstetter, R W Bendon, P S Dignan, A E Oestreich, T A Siddiqi.   

Abstract

Larsen syndrome is characterized by multiple congenital joint dislocations and flattened facies. Some cases have been familial, with both autosomal dominant and recessive patterns of inheritance. Reports of a form of Larsen syndrome, lethal in the neonatal period, are reviewed. We present a family in which recurrence of the syndrome was diagnosed prenatally, but a lethal outcome again resulted despite preparation for anticipated perinatal complications. Because of the wide clinical variation and the lack of a known metabolic defect, delineation between the various forms of Larsen syndrome is difficult. While the lethal variant appears to be a combination of the Larsen phenotype and pulmonary hypoplasia, other features noted in the lethal cases, such as abnormal palmar creases and laryngotracheomalacia, are also seen in patients with Larsen syndrome who survive.

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Year:  1991        PMID: 1716760     DOI: 10.1002/pd.1970110403

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  4 in total

1.  Larsen syndrome--lethal variety.

Authors:  M L Kulkarni; Zaheeruddin Mohammed; Preethi M Kulkarni
Journal:  Indian J Pediatr       Date:  2005-12       Impact factor: 1.967

2.  A molecular and clinical study of Larsen syndrome caused by mutations in FLNB.

Authors:  Louise S Bicknell; Claire Farrington-Rock; Yousef Shafeghati; Patrick Rump; Yasemin Alanay; Yves Alembik; Navid Al-Madani; Helen Firth; Mohammad Hassan Karimi-Nejad; Chong Ae Kim; Kathryn Leask; Melissa Maisenbacher; Ellen Moran; John G Pappas; Paolo Prontera; Thomy de Ravel; Jean-Pierre Fryns; Elizabeth Sweeney; Alan Fryer; Sheila Unger; L C Wilson; Ralph S Lachman; David L Rimoin; Daniel H Cohn; Deborah Krakow; Stephen P Robertson
Journal:  J Med Genet       Date:  2006-06-26       Impact factor: 6.318

3.  GZF1 Mutations Expand the Genetic Heterogeneity of Larsen Syndrome.

Authors:  Nisha Patel; Hanan E Shamseldin; Nadia Sakati; Arif O Khan; Ameen Softa; Fatima M Al-Fadhli; Mais Hashem; Firdous M Abdulwahab; Tarfa Alshidi; Rana Alomar; Eman Alobeid; Salma M Wakil; Dilek Colak; Fowzan S Alkuraya
Journal:  Am J Hum Genet       Date:  2017-05-04       Impact factor: 11.025

4.  Prenatal diagnosis of Larsen syndrome caused by a mutation in the filamin B gene.

Authors:  N Winer; F Kyndt; A Paumier; A David; B Isidor; M Quentin; B Jouitteau; P Sanyas; H J Philippe; A Hernandez; D Krakow; C Le Caignec
Journal:  Prenat Diagn       Date:  2009-02       Impact factor: 3.050

  4 in total

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